Vincenzo Bonifati

Overview

Best Publications

• Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

  Vincenzo Bonifati;Vincenzo Bonifati;Patrizia Rizzu;Marijke J. van Baren;Onno Schaap

  3362
  Citations

• Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

  Daniel G Healy;Mario Falchi;Sean S O'Sullivan;Vincenzo Bonifati

  1737
  Citations

• Lewy pathology in Parkinson's disease consists of crowded organelles and lipid membranes.

  Sarah H Shahmoradian;Sarah H Shahmoradian;Amanda J Lewis;Christel Genoud;Jürgen Hench

  957
  Citations

• A common LRRK2 mutation in idiopathic Parkinson's disease

  William P. Gilks;Patrick M Abou-Sleiman;Sonia Gandhi;Shushant Jain

  943
  Citations

• A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

  Abbas N;Lücking Cb;Ricard S;Dürr A

  707
  Citations

• A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

  Alessio Di Fonzo;Alessio Di Fonzo;Christan F Rohé;Joaquim Ferreira;Hsin F Chien

  663
  Citations

• A susceptibility locus for Parkinson's disease maps to chromosome 2p13

  Thomas Gasser;Bertram Müller-Myhsok;Zbigniew K. Wszolek;Ralph Oehlmann

  638
  Citations

• EFNS/MDS‐ES recommendations for the diagnosis of Parkinson's disease

  Alfredo Berardelli;Gregor Wenning;Angelo Antonini;Daniela Berg

  604
  Citations

• DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism.

  V. Bonifati;V. Bonifati;P. Rizzu;F. Squitieri;E. Krieger

  512
  Citations

• PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36

  C.M. van Duijn;M.C.J. Dekker;V. Bonifati;R.J. Galjaard

  512
  Citations

• The genetics of Parkinson's disease: Progress and therapeutic implications

  Andrew B. Singleton;Matthew J. Farrer;Vincenzo Bonifati

  443
  Citations

• FBXO7 mutations cause autosomal recessive, early-onset parkinsonian- pyramidal syndrome

  A. Di Fonzo;M.C.J. Dekker;P. Montagna;A. Baruzzi

  440
  Citations

• Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease

  Marialuisa Quadri;Antonio Federico;Tianna Zhao;Guido J. Breedveld

  435
  Citations

• ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease.

  A. Di Fonzo;H. F. Chien;M. Socal;S. Giraudo

  418
  Citations

• Early-onset parkinsonism associated with PINK1 mutations Frequency, genotypes, and phenotypes

  V. Bonifati;C. F. Rohé;G. J. Breedveld;E. Fabrizio

  412
  Citations

• Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism.

  Marialuisa Quadri;Mingyan Fang;Marina Picillo;Simone Olgiati

  346
  Citations

• Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation

  Stephen Hague;Ekaterina Rogaeva;Dena Hernandez;Cindy Gulick

  325
  Citations

• A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.

  Alessio Di Fonzo;Yah Huei Wu-Chou;Chin Song Lu;Marina Van Doeselaar

  284
  Citations

• DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.

  K. Hedrich;A. Djarmati;N. Schäfer;R. Hering

  281
  Citations

• Parkinsonism after Chronic Exposure to the Fungicide Maneb (Manganese ethylene-bis-dithiocarbamate)

  Giuseppe Meco;Vincenzo Bonifati;Nicola Vanacore;Edito Fabrizio

  274
  Citations